Sulfur hexafluoride multiple breath washin and washout outcomes in infants are not interchangeable

Physiol Meas. 2024 Nov 14;45(11). doi: 10.1088/1361-6579/ad8da4.

Abstract

Objective.Sulfur hexafluoride (SF6) multiple-breath washout (MBW) assesses ventilation inhomogeneity, as an early marker of obstructive respiratory diseases. Primary outcomes are customarily washout-derived, and it is unclear whether the preceding SF6-washin can provide similar estimates. We aimed to assess comparability of primary SF6-MBW outcomes between washin and washout phases of infant SF6-MBW data measured with the WBreath (ndd Medizintechnik AG, Zurich, Switzerland) and Spiroware (Eco Medics AG, Duernten, Switzerland) MBW-setups, respectively.Approach.We assessed mean relative differences in lung clearance index (LCI) and functional residual capacity (FRC) between the washin and washout of existing SF6-MBW data from healthy infants and infants with cystic fibrosis (CF). We assessed whether these differences exceeded the mean relative within-test between-trial differences of washout-derived outcomes, which can be attributed to natural variability. We also explored non-physiological factors using a pediatric lung simulator.Main results.LCI and FRC from washin and washout were not comparable, for both setups. The mean difference (SD) in LCI between washin and washout was 2.3(10.8)% for WBreath and -9.7(8.0)% for Spiroware, while in FRC it was -4.7(8.4)% for WBreath and -2.3(9.7)% for Spiroware. These differences exceeded the within-test between-trial differences in washout-derived outcomes. Outcomes from washin and washout were also not comparable in a pediatric lung simulator.Significance.Outcomes of the washin and washout were not comparable due to an interplay of physiological and non-physiological factors, and cannot be used interchangeably.

Keywords: SF6-multiple-breath washout; cystic fibrosis; lung physiology; pediatric lung disease; pulmonary function test.

MeSH terms

  • Breath Tests / methods
  • Cystic Fibrosis* / metabolism
  • Cystic Fibrosis* / physiopathology
  • Female
  • Humans
  • Infant
  • Male
  • Respiration
  • Respiratory Function Tests
  • Sulfur Hexafluoride*

Substances

  • Sulfur Hexafluoride